Alprazolam - 63629-3308-4 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 63629-3308
Proprietary Name: Alprazolam
Non Proprietary Name: alprazolam
Active Ingredient(s): 2    mg/1 & nbsp;   alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 63629-3308
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018276
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19811016

Package Information of Alprazolam

Package NDC: 63629-3308-4
Package Description: 100 TABLET in 1 BOTTLE (63629-3308-4)

NDC Information of Alprazolam

NDC Code 63629-3308-4
Proprietary Name Alprazolam
Package Description 100 TABLET in 1 BOTTLE (63629-3308-4)
Product NDC 63629-3308
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19811016
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Bryant Ranch Prepack
Substance Name ALPRAZOLAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information